Cross-sectional characterization of HIV-1 env compartmentalization in cerebrospinal fluid over the full disease course

AIDS. 2009 May 15;23(8):907-15. doi: 10.1097/QAD.0b013e3283299129.

Abstract

Objectives: To characterize HIV-1 env compartmentalization between cerebrospinal fluid (CSF) and peripheral blood plasma over all stages of the HIV-1 disease course, and to determine the relationship between the extent of CSF HIV-1 env compartmentalization and clinical neurologic disease status.

Design: Paired blood plasma and CSF specimens were collected from 66 HIV-infected patients cross-sectionally representing all major clinical stages relating to HIV-associated neurologic disease, including primary infection, asymptomatic chronic infection, chronic infection with minor global impairment, and immune deficiency with HIV-associated dementia.

Methods: Heteroduplex tracking assays and bulk sequence analysis targeting the V1/V2, C2-V3, and V4/V5 regions of env were performed to characterize the genetic makeup of complex HIV-1 populations in the cross-sectional blood plasma and CSF specimens. The levels of blood plasma/CSF env compartmentalization were quantified and compared across the different clinical stages of HIV-1 neurologic disease.

Results: Blood plasma/CSF env compartmentalization levels varied considerably by disease stage and were generally consistent across all three regions of env characterized. Little or no compartmentalization was observed in non-impaired individuals with primary HIV-1 infection. Compartmentalization levels were elevated in chronically infected patients, but were not significantly different between mildly impaired and non-impaired patients. Patients with HIV-associated dementia showed significantly greater blood plasma/CSF env compartmentalization relative to other groups.

Conclusion: : Increased CSF compartmentalization of the HIV-1 env gene, which may reflect independent HIV-1 replication and evolution within the central nervous system, is specifically associated with HIV-associated dementia and not the less severe forms of HIV-1 neurologic disease.

Publication types

  • Multicenter Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • AIDS Dementia Complex / complications
  • AIDS Dementia Complex / metabolism
  • California
  • Chronic Disease
  • Cross-Sectional Studies
  • Disease Progression
  • Genes, env*
  • HIV Infections / blood
  • HIV Infections / cerebrospinal fluid*
  • HIV Infections / complications
  • HIV-1 / genetics*
  • Humans
  • Nervous System Diseases / blood
  • Nervous System Diseases / cerebrospinal fluid*
  • Nervous System Diseases / complications
  • North Carolina
  • San Francisco